PSI CRO

HQ
Zug, Zug, CHE
1,939 Total Employees
Year Founded: 1995

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Jobs at PSI CRO

Search the 54 jobs at PSI CRO

Recently posted jobs

Pharmaceutical
The Site Technology Specialist provides technical support and expertise for clinical sites, assists in the design and implementation of study-related technologies, coordinates data collection, and provides training and documentation support for project teams.
2 Days Ago
USA
Remote
Pharmaceutical
The Lead Data Manager is responsible for managing all data activities in clinical trials, serving as the primary point of communication between project teams and clients, coordinating data management tasks, developing documentation, performing data review and reconciliation, and training junior staff.
Pharmaceutical
The Site Contract Specialist is responsible for negotiating site agreements and budgets, preparing customized agreements, tracking negotiations, and filing executed agreements. This role ensures alignment with site activation plans and updates all functions related to the site contracting process.
2 Days Ago
Almaty, KAZ
Pharmaceutical
The Freelance CRA role involves coordinating clinical trials, supporting site activation, monitoring patient enrollment, and ensuring compliance with study protocols. Responsibilities include liaising between sponsors and sites, preparing for monitoring visits, tracking documents, and participating in audits or inspections.
Pharmaceutical
The Study Startup Specialist I will support site activation processes, assist with feasibility research, maintain tracking systems, manage site agreement documents, and ensure timely communication with project teams and sites during the startup phase.
3 Days Ago
Vienna, AUT
Pharmaceutical
The Central Monitoring Manager at PSI will lead the implementation of risk-based monitoring in clinical studies, manage centralized monitoring activities, and develop study-specific plans. The role involves analyzing key risk indicators, communicating with cross-functional teams, and presenting findings to clients, ensuring patient safety and data integrity.
3 Days Ago
Tallinn, Harju maakond, EST
Remote
Pharmaceutical
The Central Monitoring Manager will lead the implementation of risk-based monitoring approaches for clinical studies, ensuring patient safety and data integrity. Responsibilities include managing risk management, participating in platform selection, conducting centralized monitoring, and developing study-specific plans.
3 Days Ago
Rīga, LVA
Remote
Pharmaceutical
The Central Monitoring Manager will lead the implementation of risk-based monitoring in clinical studies, facilitate ongoing risk management, analyze data, and present findings to study teams and clients. The role requires strong communication skills and the ability to work with complex data while ensuring patient safety and data integrity.
3 Days Ago
Munich, Bavaria, DEU
Remote
Pharmaceutical
The Central Monitoring Manager will lead the implementation of the risk-based monitoring approach for clinical studies, ensuring patient safety and data integrity. Responsibilities include developing study plans, performing centralized monitoring, managing issues in a team environment, and contributing to proposal meetings with insights on risk management services.
3 Days Ago
Vilnius, Vilniaus apskritis, LTU
Remote
Pharmaceutical
The Central Monitoring Manager will lead the implementation of risk-based monitoring for clinical studies, oversee centralized monitoring activities, analyze risk indicators, and present findings to teams and clients, ensuring patient safety and data integrity.
3 Days Ago
2 Locations
Remote
Pharmaceutical
The Central Monitoring Manager will lead the implementation of risk-based monitoring for clinical studies, ensuring patient safety and maintaining data integrity. Responsibilities include risk management, centralized monitoring, presenting analysis results, and managing data review activities while communicating challenges and solutions effectively.
3 Days Ago
Warsaw, Warszawa, Masovian, POL
Remote
Pharmaceutical
The Central Monitoring Manager will lead risk-based monitoring for clinical studies, manage centralized monitoring activities, present analysis results, develop study-specific plans, and coordinate with various teams to enhance data integrity and patient safety.
3 Days Ago
Taipei, TWN
Pharmaceutical
As an Associate Legal Counsel at PSI, you will support legal needs primarily related to clinical research contracts. Responsibilities include reviewing and drafting contracts, providing legal advice on compliance and legislation, researching legal matters, and ensuring policy compliance.
5 Days Ago
Bucharest, București, ROU
Pharmaceutical
As a Site Management Associate I, you will support clinical research projects by managing communication, maintaining documentation, coordinating project workflows, ensuring regulatory compliance, and overseeing trial master files. You will assist in the organization of team meetings and ensure effective safety information exchange with investigative sites.
5 Days Ago
Oxford, Oxfordshire, England, GBR
Pharmaceutical
The Site Management Associate will start a career in clinical research, managing communication, systems, and documents. Responsibilities include maintaining databases, managing large volumes of documents, coordinating site-specific queries, preparing meeting materials, and facilitating communications with staff and external parties.
6 Days Ago
Toronto, ON, CAN
Pharmaceutical
As a Junior Accountant, you will manage customer invoicing, follow up on payments, reconcile accounts, and maintain customer data. You will also assist with processing payments and contribute to improving accounts receivable processes.
6 Days Ago
Global Village, Shilphata, Thane, Maharashtra, IND
Remote
Pharmaceutical
The Freelance Content Creator will develop and implement content strategies to enhance employer branding and attract talent in clinical research. Responsibilities include creating diverse content, managing social media, designing campaigns, collaborating with HR, and analyzing content performance.
6 Days Ago
Global Village, Shilphata, Thane, Maharashtra, IND
Remote
Pharmaceutical
The Freelance Recruiter will identify, attract, and hire talent for clinical research. Responsibilities include sourcing candidates, engaging them, collaborating with the talent manager, coordinating interviews, and managing candidate databases, all while working independently and maintaining strong communication skills.
6 Days Ago
Kyiv, Kiev, UKR
Pharmaceutical
The Associate Legal Counsel role involves providing legal support focused on local legal matters in Ukraine, including reviewing and drafting contracts, providing legal advice to various departments, ensuring compliance with company policies, and assisting with clinical trial agreements.
Pharmaceutical
The Site Management Associate I provides support to clinical research projects by managing communication, documentation, and clinical supplies. Responsibilities include data exchange, coordinating audits and inspections, maintaining Trial Master Files, and offering administrative project support.